
Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(2,968 products)
- Antibiotic(922 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(711 products)
- HBV(177 products)
- HIV Protease(451 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5863 products of "Microbiology/Virology"
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RyRs activator 2
CAS:<p>RyRs activator 2: potent ranibulin receptor stimulant, 30% larvicidal activity, equals chlorfenvinphos, outperforms cyanobenzamide.</p>Formula:C23H18Cl2F3N5O2Color and Shape:SolidMolecular weight:524.32PTC725
CAS:<p>PTC725 is a selective HCV 1b replicons inhibitor. It has been shown to target the nonstructural protein 4B.</p>Formula:C23H18F4N6O2SPurity:98%Color and Shape:SolidMolecular weight:518.49WQ 2743
CAS:<p>WQ 2743 is a potent agent of antimicrobial.</p>Formula:C19H15BrF3N5O3Purity:98%Color and Shape:SolidMolecular weight:498.25UNC2170 maleate
CAS:<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Formula:C14H21BrN2OC4H4O4Color and Shape:SolidMolecular weight:429.31Cefteram
CAS:<p>Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil.</p>Formula:C16H17N9O5S2Color and Shape:SolidMolecular weight:479.49AZ-27
CAS:<p>AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.</p>Formula:C36H35N5O4SColor and Shape:SolidMolecular weight:633.76(E)-LHF-535
CAS:<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Formula:C27H28N2O2Purity:98%Color and Shape:SolidMolecular weight:412.52DHX9-IN-4
CAS:<p>DHX9-IN-4 is an ATP-dependent RNA helicase DHX9 inhibitor used in cancer research.</p>Formula:C21H22ClN5O4S2Purity:98.12%Color and Shape:SolidMolecular weight:508.01Murabutide
CAS:<p>Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,</p>Formula:C23H40N4O11Color and Shape:SolidMolecular weight:548.58Bio-AMS
CAS:<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Formula:C20H29N9O7S2Color and Shape:SolidMolecular weight:571.63Variculanol
CAS:<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Formula:C25H40O2Color and Shape:SolidMolecular weight:372.58RAD51-IN-4
CAS:<p>RAD51-IN-4, a potent RAD51 inhibitor, may be useful in researching mitochondrial defect-related conditions.</p>Formula:C31H34FN5O5S2Color and Shape:SolidMolecular weight:639.76SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Formula:C30H36N4O7Color and Shape:SolidMolecular weight:564.63Flurofamide
CAS:<p>Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.</p>Formula:C7H9FN3O2PPurity:96.01% - 98%Color and Shape:SolidMolecular weight:217.14Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C20H20Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:451.37MurA-IN-4
CAS:<p>MurA-IN-4 exhibits antibacterial properties as a MurA inhibitor, impeding the synthesis of bacterial cell walls [1].</p>Formula:C8H12ClNO3Color and Shape:SolidMolecular weight:205.64Myxopyronin A
CAS:<p>Myxopyronin A is an inhibitor of bacterial RNA polymerase.</p>Formula:C23H31NO6Purity:98%Color and Shape:SolidMolecular weight:417.5LS-BF1
CAS:<p>LS-BF1: Stable, low-toxic antimicrobial peptide targeting ESKAPE pathogens via cell membrane disruption, effective in mouse infection model.</p>Formula:C107H166N28O15Color and Shape:SolidMolecular weight:2084.64(+)-Thienamycin
CAS:<p>(+)-Thienamycin, a powerful broad-spectrum antibacterial and β-lactamase inhibitor, is isolated from Streptomyces cattleya [1].</p>Formula:C11H16N2O4SColor and Shape:SolidMolecular weight:272.32JNJ4796
CAS:<p>JNJ4796 is an oral fusion inhibitor that neutralizes influenza A group 1 by blocking HA-mediated fusion, mimicking bnAbs.</p>Formula:C28H27N9O3Purity:98%Color and Shape:SolidMolecular weight:537.57SARS-CoV-2-IN-62
CAS:<p>SARS-CoV-2-IN-62 (Compound R3b) effectively inhibits SARS-CoV-2 replication in Vero E6 and Calu-3 cells, demonstrating low cytotoxicity and EC50 values of 2.97</p>Formula:C17H21N3O3SePurity:98%Color and Shape:SolidMolecular weight:394.33NCI-B16
CAS:<p>NCI-B16 is a small-molecule RNA binder that inhibits HCV (hepatitis C virus) replication [1].</p>Formula:C27H26N8O4Color and Shape:SolidMolecular weight:526.55Amoxicillin-clavulanate potassium
CAS:<p>Amoxicillin-clavulanate potassium is an orally administered antibiotic and combination agent indicated for various bacterial infections.</p>Formula:C24H27KN4O10SPurity:98%Color and Shape:SolidMolecular weight:602.66Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Formula:C20H16O5Color and Shape:SolidMolecular weight:336.34Du011
CAS:<p>Du011 is a biogenesis inhibitor of the E.</p>Formula:C20H15F2NO4SColor and Shape:SolidMolecular weight:403.4ThrRS-IN-3
<p>ThrRS-IN-3: Potent inhibitor of Salmonella enterica ThrRS, IC50 = 19 nM, Kd = 34 nM, with antibacterial effects.</p>Formula:C31H30Cl2N6O5Color and Shape:SolidMolecular weight:637.51BRL44385
CAS:<p>BRL44385 is an effective and selective inhibitor of the replication of HSV-1 and HSV2, Epstein-Barr virus (EBV), and varicella-zoster virus (VZV).</p>Formula:C8H11N5O3Purity:98%Color and Shape:SolidMolecular weight:225.2MC-VC-PAB-Cyclohexanediamine-Thailanstatin A
CAS:<p>MC-VC-PAB-Cyclohexanediamine-Thailanstatin A is a spliceostatin analog and a drug-linker conjugate for antibody-drug conjugates (ADC), comprising the cytotoxic</p>Formula:C63H91N9O16Purity:98%Color and Shape:SolidMolecular weight:1230.45HBV-IN-41
CAS:<p>HBV-IN-41 (compound 45) is a potent, orally active inhibitor of Hepatitis B Virus (HBV), exhibiting an EC50 value of 0.027μM [1].</p>Formula:C18H19ClFN5O3Purity:98%Color and Shape:SolidMolecular weight:407.83H3B-968
CAS:<p>H3B-968 is a potent inhibitor of Werner syndrome protein (WRN) with an IC50 of approximately 10 nM, effectively targeting its helicase, ATPase, and exonuclease</p>Formula:C22H18F6N4O4SPurity:98%Color and Shape:SolidMolecular weight:548.46SARS-CoV-2/MERS Mpro-IN-2
<p>SARS-CoV-2/MERS Mpro-IN-2 is a potent inhibitor of the main proteases of SARS-CoV-2 and MERS, demonstrating IC50 values of 0.21 and 0.07 µM, respectively.</p>Formula:C28H30Cl2N4O6Color and Shape:SolidMolecular weight:589.47BAY-Y 3118
CAS:BAY-Y 3118, a new chlorofluoroquinolone, has antimicrobial activity.Formula:C20H21ClFN3O3Color and Shape:SolidMolecular weight:405.85CDD-1819
CAS:<p>CDD-1819, a non-covalent and non-peptide compound, serves as a potent SARS-CoV-2 Mpro inhibitor, exhibiting a K i value of 5 nM.</p>Formula:C35H31N5O2Purity:98%Color and Shape:SolidMolecular weight:553.65CGP 20376
CAS:<p>CGP 20376: Benzothiazole anthelmintic, modulates eosinophil burst, antifibrillatory, dose-dependent effects.</p>Formula:C16H20N2O3S3Purity:95.11%Color and Shape:SolidMolecular weight:384.54Mtb-IN-4
CAS:<p>Mtb-IN-4 (compound 17h) is a non-toxic isoxazole that exhibits anti-Mycobacterium tuberculosis (Mtb) activity, with an IC50 value of 0.70 μM.</p>Formula:C24H18N2O4SColor and Shape:SolidMolecular weight:430.485,6,7,8-Tetrahydro-8-deazahomofolic acid
CAS:<p>5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Formula:C21H26N6O6Color and Shape:SolidMolecular weight:458.47Phenethicillin sodium
CAS:<p>Phenethicillin sodium (α-Phenoxyethylpenicillin) is a penicillin-class antibiotic that exhibits antimicrobial activity [1].</p>Formula:C17H19N2NaO5SColor and Shape:SolidMolecular weight:386.4Phylloflavan
CAS:<p>Phylloflavan, an antileishmanial compound, exhibits an intracellular half maximal effective concentration (EC50) of 3.2 nM in RAW 264.7 cells and inhibits the</p>Formula:C26H26O10Purity:98%Color and Shape:SolidMolecular weight:498.48L-742001 Hydrochloride
CAS:<p>L-742001 Hydrochloride is an RNA polymerase inhibitor.</p>Formula:C23H25Cl2NO4Color and Shape:SolidMolecular weight:450.36Y18501
CAS:<p>Y18501, an oxysterol-binding protein (OSBPI) inhibitor structurally akin to Oxathiapiprolin, demonstrates potent inhibition against Phytophthora spp.</p>Formula:C27H26F2N6O2SColor and Shape:SolidMolecular weight:536.6NSC309401
CAS:<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor, displaying potency with an IC50 value of 189 nM and a dissociation constant (KD) of 14.57 nM [1].</p>Formula:C17H16N6Color and Shape:SolidMolecular weight:304.35N-(3-Oxobutanoyl)-L-homoserine lactone
CAS:<p>N-(3-Oxobutanoyl)-L-homoserine lactone (3-oxo-C4-HSL) serves as an autoregulator for carbapenem antibiotic biosynthesis in Erwinia carotovora ATCC 39048 and induces the expression of rhiI in R. leguminosarum [1].</p>Formula:C8H11NO4Color and Shape:SolidMolecular weight:185.18HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Formula:C9H10F2N2O5Purity:98%Color and Shape:SolidMolecular weight:264.18YH-53
CAS:<p>YH-53: potent inhibitor for SARS-CoV-1 (Ki=6.3 nM) & SARS-CoV-2 3CLpro (Ki=34.7 nM); hinders SARS-CoV-2 replication; aids COVID-19 research.</p>Formula:C30H33N5O5SColor and Shape:SolidMolecular weight:575.68NNRTIs-IN-1
CAS:<p>NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with notable anti-resistance efficacy, effectively inhibiting both the wild-type</p>Formula:C28H22N6O3Color and Shape:SolidMolecular weight:490.51D1N8
CAS:<p>D1N8 is a potent inhibitor of the SARS-CoV-2 3CL protease, displaying an IC50 value of 0.44 μM and a CC50 value of greater than 20 μM.</p>Formula:C19H14ClN5O3Purity:98%Color and Shape:SolidMolecular weight:395.8Antibiofilm agent-1
CAS:<p>Antibiofilm Agent-1, as detailed in WO2017011725A1 (compound 17) [1], serves as an antibacterial agent effective against Gram-positive pathogens.</p>Formula:C11H5Br2Cl2NO2Color and Shape:SolidMolecular weight:413.88Cochliodone A
CAS:<p>Cochliodone A, a bioactive compound isolated from the deep-sea fungus Chaetomium sp., exhibits both antibacterial and anticancer properties.</p>Formula:C34H38O12Color and Shape:SolidMolecular weight:638.66GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Formula:C36H46ClN3O3Color and Shape:SolidMolecular weight:604.22U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Formula:C28H52N8O6Purity:98%Color and Shape:SolidMolecular weight:596.76

